hey everyone, i want to use ROSE to identify super enhancer and to see if there is difference in the super enhancer after some treatment in lung cancer cell line i see that this is the typical use:

[user@cn3107 ~]$ ROSE_main.py -h 
Usage: ROSE_main.py [options] -g [GENOME] -i [INPUT_REGION_GFF] -r [RANKBY_BAM_FILE] -o [OUTPUT_FOLDER] [OPTIONAL_FLAGS]

Options:
  -h, --help            show this help message and exit
  -i INPUT, --i=INPUT   Enter a .gff or .bed file of binding sites used to
                        make enhancers
  -r RANKBY, --rankby=RANKBY
                        bamfile to rank enhancer by
  -o OUT, --out=OUT     Enter an output folder
  -g GENOME, --genome=GENOME
                        Enter the genome build (MM9,MM8,HG18,HG19,MM10,HG38)
  -b BAMS, --bams=BAMS  Enter a comma separated list of additional bam files
                        to map to
  -c CONTROL, --control=CONTROL
                        bamfile to rank enhancer by
  -s STITCH, --stitch=STITCH
                        Enter a max linking distance for stitching
  -t TSS, --tss=TSS     Enter a distance from TSS to exclude. 0 = no TSS
                        exclusion

i do have the bam files but i didn't understand how to get the enhancer file in gf/bed format and also how to install this program on my computer. i would like to get any explanation